chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2111835770111835771TC37GENIChomozygous553844159
2111835791111835792GT38GENIChomozygous553844160
2111835826111835827AAC36GENIChomozygous702322394
2111835908111835909CT40GENIChomozygous553844161
2111836059111836060TC44GENIChomozygous553844162
2111836218111836219TG37GENIChomozygous553844163
2111836860111836861TA42GENIChomozygous553844164
2111837033111837034CT28GENIChomozygous553844165
2111837055111837056TC29GENIChomozygous553844166
2111837056111837057CT29GENIChomozygous553844167
2111837531111837532AC41GENIChomozygous553844168
2111837554111837555TC39GENIChomozygous553844169
2111837855111837856GA28GENIChomozygous553844170
2111838008111838009TG30GENIChomozygous553844171
2111838338111838339TC32GENIChomozygous553844172
2111838463111838464TC26GENIChomozygous553844173
2111838660111838661CA30GENIChomozygous553844174
2111839273111839274GT17GENIChomozygous554951965
2111839692111839693TC26GENIChomozygous553844175
2111839973111839974CT25GENIChomozygous553844176
2111840740111840741TC36GENIChomozygous553844177
2111841130111841131CT29GENIChomozygous553844178
2111841151111841152TG24GENIChomozygous553844179
2111841706111841707TC30GENIChomozygous553844180
2111841936111841937CT19GENICpossibly homozygous553844181
2111842216111842217CA35GENIChomozygous553844182